首页> 外文期刊>Therapeutic Drug Monitoring >Development and Validation of an Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry Method for the Concurrent Measurement of Gabapentin, Lamotrigine, Levetiracetam, Monohydroxy Derivative of Oxcarbazepine, and Zonisamide Concentrations in Serum in a Clinical Setting
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Development and Validation of an Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry Method for the Concurrent Measurement of Gabapentin, Lamotrigine, Levetiracetam, Monohydroxy Derivative of Oxcarbazepine, and Zonisamide Concentrations in Serum in a Clinical Setting

机译:超高效液相色谱 - 串联质谱法的发展与验证,用于临床环境中氧化碱,氧化碱,氧化胺衍生物的单羟基,单羟基衍生物,血清中血清中的血清中的单羟基衍生物

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摘要

Background: Therapeutic drug monitoring of antiepileptic drugs (AEDs) is often necessary to prevent associated destructive toxicities. Tandem mass spectrometry (MS/MS) with stable-isotope- labeled internal standards is considered the gold standard for the measurement of AEDs. This study presents the development and validation of a clinical ultra-performance liquid chromatography- MS/MS method for the concurrent measurement of gabapentin, lamotrigine, levetiracetam, monohydroxy derivative of oxcarbazepine, and zonisamide in human serum.
机译:背景:抗癫痫药物(AED)的治疗药物监测通常是必要的,以防止相关的破坏性毒性。 具有稳定同位素标记的内标的串联质谱(MS / MS)被认为是测量AED的金标准。 本研究介绍了临床超高效液相色谱 - MS / MS方法的开发和验证,用于加布帕坦,氧化嗪,Levetiracetam,Oxcarbazepine的单羟基衍生物和人血清中的Zonisamide。

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